HYDROPS-ECTOPIC CALCIFICATION - MOTH-EATEN SKELETAL DYSPLASIA (GREENBERG DYSPLASIA) - PRENATAL-DIAGNOSIS AND FURTHER DELINEATION OF A RARE GENETIC DISORDER

被引:32
作者
CHITAYAT, D
GRUBER, H
MULLEN, BJ
PAUZNER, D
COSTA, T
LACHMAN, R
RIMOIN, DL
机构
[1] UNIV TORONTO, TORONTO GEN HOSP, PRENATAL DIAG PROGRAM, TORONTO M5G 1L7, ONTARIO, CANADA
[2] UNIV TORONTO, MT SINAI HOSP, DEPT PATHOL, TORONTO M5G 1X5, ONTARIO, CANADA
[3] UNIV TORONTO, MT SINAI HOSP, DEPT OBSTET & GYNECOL, TORONTO M5G 1X5, ONTARIO, CANADA
[4] CEDARS SINAI MED CTR, DEPT PEDIAT, LOS ANGELES, CA 90048 USA
[5] UNIV CALIF LOS ANGELES, HARBOR MED CTR, TORRANCE, CA USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 47卷 / 02期
关键词
FETAL; SKELETAL DYSPLASIA; LETHAL; INHERITED; POLYDACTYLY; CYSTIC HYGROMA; AUTOSOMAL RECESSIVE;
D O I
10.1002/ajmg.1320470226
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
An offspring of consanguineous parents of East-Indian origin was found prenatally to have hydrops fetalis, short limb dwarfism, polydactyly and chondro-osseous changes consistent with Greenberg hydrops-ectopic calcification-moth-eaten skeletal dysplasia (HEM) dysplasia. The radiological changes include platyspondyly with multiple extra ossification centers, extraneous calcification in the ribs, sternum, pelvis, and epiphysis, and moth-eaten long bones. The histopathological changes included chondrocytes with dilated rough endoplasmic reticulum and inclusion bodies with homogeneous material of intermediate electron density. These findings further delineate the spectrum of this rare autosomal recessive skeletal dysplasia. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:272 / 277
页数:6
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